| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17933269-17933293 | Rare:7 | ||||
| chr19:18001041-18001347 | Common:2; Rare:77 | ||||
| chr19:18007991-18008233 | Common:5; Rare:85 | ||||
| chr19:18086604-18086877 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr19:18086885-18087132 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr19:18087153-18087235 | Common:1; Rare:18 | ||||
| chr19:18097579-18097837 | Common:1; Rare:53 | ||||
| chr19:18098611-18099146 | Rare:86 | ||||
| chr19:18099148-18099229 | Rare:17 | ||||
| chr19:18099231-18099690 | Common:1; Rare:89 | ||||
| chr19:18110436-18110593 | Common:1; Rare:21 | ||||
| chr19:18152401-18152777 | Common:1; Rare:101 | ||||
| chr19:18152866-18153319 | Common:2; Rare:133 | ||||
| chr19:18161296-18161486 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr19:18173478-18173894 | Common:3; Rare:84 |